Has your friend or relative received a diagnosis for their child, and you want to know how to help?

Are you a parent feeling overwhelmed and at times isolated by your own child’s needs?

Right now there is such a gap between parents of disabled kids and the “villages” we look to for support.

In 2018, I started this website as a way to process my thoughts and emotions after my young son JB was diagnosed with a genetic syndrome.

By sharing my experience, I want to bridge that divide through honest conversation about friendship, parenting, disability, and inclusion.